872513-93-4Relevant academic research and scientific papers
A one pot, metathesis-hydrogenation sequence for the selective formation of carbon-carbon bonds
Robinson, Andrea J.,Elaridi, Jomana,Patel, Jim,Jackson, W. Roy
, p. 5544 - 5545 (2005)
A combination of homogeneous hydrogenation and metathesis reactions allows highly efficient, stepwise chemo- and stereo-selective formation of three separate 2,7-diaminosuberic acid derivatives in a single pot without isolation of intermediates. The Royal
Methods for the synthesis of dicarba bridges in organic compounds
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, (2015/11/17)
The present invention relates to methods for forming dicarba bridges in organic compounds. This involves the use of a pair of complementary metathesisable groups on the organic compound, and subjecting the compound to cross-metathesis under microwave radiation conditions. In an alternative, the compounds contain a turn-inducing group between the pair of cross-metathesisable groups to facilitate the cross-metathesis.
An efficient protocol for the cross-metathesis of sterically demanding olefins
Wang, Zhen J.,Jackson, W. Roy,Robinson, Andrea J.
supporting information, p. 3006 - 3009 (2013/07/26)
Cross-metathesis of a wide range of previously unreactive, sterically demanding alkenes can be achieved in fair to excellent yield using a commercially available catalyst by a facile strategy involving reversal of steric preference.
Conotoxin analogues and methods for synthesis of intramolecular dicarba bridge-containing peptides
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Page/Page column 72; 54; 28, (2010/11/28)
According to the present invention, there is provided a range of new conotoxin derivatives and methods for synthesizing these analogues and other intramolecular dicarba bridge-containing peptides, including dicarba-disulfide bridge-containing peptides.
